An alkene (X) on ozonolysis gives propanal an | vedclass

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(A) Ozonolysis of an alkene involves the cleavage of the double bond to form two carbonyl compounds.Given products are $CH_3-CH_2-CHO$ (propanal) and

Vedclass · Accepted Answer

Pent$-2-$ene

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(A) Ozonolysis of an alkene involves the cleavage of the double bond to form two carbonyl compounds.Given products are $CH_3-CH_2-CHO$ (propanal) and $CH_3-CHO$ (ethanal).By removing the oxygen atoms from the carbonyl groups and joining the carbon atoms with a double bond,we get:$CH_3-CH_2-CH=CH-CH_3$.The structure corresponds to $Pent-2-ene$.Therefore,the correct option is $A$.

An alkene $(X)$ on ozonolysis gives propanal and ethanal. What is $X$?

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